A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205232



Internal ID20772272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16751009..17002124hg38UCSC Ensembl
chr20:16731654..16982769hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38251116
hg19251116
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6516080
Supporting Variants
Samples
Known GenesOTOR
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205232
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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